Role at a glance
- Job function
-
Legal & Compliance Compliance & Regulatory Affairs
- Salary
- Not Disclosed
- Location
- TS, Indiana, United States
- Employment
- Full-time
Spotted an issue?
We’ll check it against the original posting.
Role Summary
The Regulatory Specialist supports regulatory strategy, submissions, and portfolio-related activities. The role also contributes to regulatory intelligence, cross-functional reporting, and regulatory analytics.
What You'll Do
- Maintain SharePoint materials and support GRT member transitions.
- Support regulatory submissions, including planning deliverables, preparing Module 1 documents, requesting health authority certificates,...
- Upload and remediate documents for product divestitures and asset integration, and gather information for product deletion strategies...
- Coordinate health authority query and shortage notification activities, including scheduling meetings, preparing response templates, and...
- Prepare regulatory analytics and monthly dashboards, and liaise cross-functionally on milestone reports.
Generated from the employer's posting. Verify important details before applying.
View full posting
Original job description
Content provided by the employer
Original job description
Content provided by the employer
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Job Description
Position Responsibilities
Responsibilities include but not limited to:
- SharePoint Maintenance Activities; Support GRT member transition by setting up transition form (operational)
Execution of Regulatory Strategy
- Liaise cross-functionally to generate periodic internal milestone report
Regulatory Intelligence
- Performs simple analyses as directed
Global Regulatory Submissions Support
- Support planning and managing timely deliverable of critical regulatory deliverables (registration samples) and various Module 1 documents for ex-US,ex-EU countries
- Request certificates from respective Health Authority (FDA, EMA, Swiss Medic) and manage notification process
- Shipping of documents, as required
- Admin- scanning, copying, shipping label
- undefined
- Product Divestiture: Upload relevant documents into the Virtual Data Room (VDR) for potential buyers
- Product Deletions: Gather information from the Country Regulatory Managers for Product Deletions Strategy
- Tracks deletion notifcations to country Reg HA
- Asset Integration: Upload incoming documents to the BMS systems, ensure correct update of meta data; Remediation of documents, as directed
HA queries / Shortage Notifications
- Schedule RRT meetings and communicate timelines
- Set up response templates to ensure submission readiness
- Submission of responses for publishing
Analytics / Compliance Activities
Support preparation of GRS analytics and monthly dashboards, eg submission, Approvals, key achievements, miles stones
Technology & Analytics Adoption – Embrace and apply analytics and technologies to the BoW activities and process.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
How We Work
Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.
About the company
Bristol Myers Squibb
Large Enterprise
Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.